Evidence map›Paper›PMID 36769639›Full record

ArticleJournal of clinical medicine2023

Clinicopathological and Treatment Patterns of Combined Small-Cell Lung Carcinoma with Future Insight to Treatment: A Population-Based Study.

Asad Ullah, Omer Saeed, Nabin Raj Karki, Mya Goodbee, Abdul Qahar Khan Yasinzai, Abdul Waheed, Saleh Heneidi, Anish Thomas, Nagla Abdel Karim, Joyce Johnson and 2 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Asad UllahDepartment of Pathology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-9435-9625
Omer SaeedDepartment of Pathology, Indiana School of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Nabin Raj KarkiDepartment of Hematology and Oncology, University of South Alabama, Mobile, AL 36688, USA.ORCID 0000-0001-6449-8109
Mya GoodbeeMedical College of Georgia, Augusta University, Augusta, GA 30912, USA.
Abdul Qahar Khan YasinzaiDepartment of Medicine, Bolan Medical College, Quetta 83700, Pakistan.ORCID 0000-0002-8146-1620
Abdul WaheedDepartment of Surgery, San Joaquin General Hospital, San Joaquin, CA 95231, USA.ORCID 0000-0002-9992-6051
Saleh HeneidiDepartment of Molecular Pathology, Cedars Sinai Medical Center, Los Angeles, CA 90048, USA.
Anish ThomasDepartment of Hematology and Oncology, National Institute of Health (NIH), Bethesda, MA 20814, USA.
Nagla Abdel KarimDepartment of Hematology and Oncology, Inova Schar Cancer Institute, Fairfax, VA 22031, USA.
Joyce JohnsonDepartment of Pathology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Jaydira Del RiveroDepartment of Hematology and Oncology, National Institute of Health (NIH), Bethesda, MA 20814, USA.ORCID 0000-0001-9710-4030
Jaffar KhanDepartment of Pathology, Indiana School of Medicine, Indiana University, Indianapolis, IN 46202, USA.

Funding

Exploiting DNA Replicative Stress for Novel Small Cell Lung Cancer TherapiesZIABC011793 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI THOMAS, ANISH · 2018 to 2025
$16.4M
6 · The paper itself

Abstract

backgroundPrimary lung cancer is the most common cause of cancer-related mortality in the United States (US). Approximately 90% of lung cancers are associated with smoking and the use of other tobacco products. Based on histology, lung cancers are divided into small-cell lung carcinomas (SCLCs) and non-small-cell lung carcinomas (NSCLCs). Most SCLCs are of the pure subtype, while the rare combined SCLCs contain elements of both small-cell and non-small-cell morphologies. This study sought to evaluate the demographics, clinical factors, molecular abnormalities, treatment approaches, and survival outcomes with combined SCLC and NSCLCs. MATERIALS AND

methodsData on 2126 combined SCLC patients was extracted from the Surveillance Epidemiology and End Result (SEER) database from 2000 to 2018. Data extracted for analyses included age, sex, race, tumor size, tumor location, metastasis status, stage at diagnosis, treatment received, and treatment outcomes. Multivariate analysis was performed using Statistical Product and Service Solutions (SPSS) software.

resultsThe patients had a median age of 68 years; 43.9% of the patients were female and 56.1% were male; 84.5% were White and 11.7% were African Americans. The majority of patients had a poorly differentiated disease at 29.6%; 17% were undifferentiated, 3.2% were moderately differentiated, and 0.8% were well differentiated. Chemotherapy was the most common treatment modality (45.3%); 17% underwent surgery only, 10.3% underwent surgery followed by adjuvant chemotherapy, and 10% underwent radiation after surgery. Five-year cancer-specific survival was 15.2% with surgery alone, and combined surgery and chemotherapy provided the highest percentages (38.3% and 34.7%, respectively). Females had significantly higher 1- and 5-year cancer-specific survival rates compared to males (59.3% and 29.9% vs. 48.0% and 23.7, respectively;

conclusionCombined SCLC is overall very rare. However, the frequency of presentation with combined SCLC is on the rise, in part due to improvements in diagnostic techniques. Despite advances in therapies, treating combined SCLC is challenging, and novel therapies are not utilized, owing to low rates of targetable mutations. Combined SCLC has higher survival rates if well differentiated.

Indexed as

chemotherapycombined small cellhistologylung cancermolecular changes

Identifiers

PMID36769639
PMCPMC9918142

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.